Disease #00227 (ARVD10 (ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10), OMIM:610193)

Official abbreviation	ARVD10
Name	ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 10
OMIM ID	610193
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	Autosomal dominant
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	DSG2
Associated tissues	-
Disease features	-
Remarks	-
Date created	2025-10-06 07:45:27 +00:00 (UTC)
Date last edited	N/A

MVZ für Humangenetik Regensburg